Ammonia → HCID 59456908, compound

HRID 1362209Notes

Reaction equation

HRID 1362209 reaction equation
[O:1]=[C:2]1[CH2:6][CH2:5][C:4](=[O:7])[N:3]1[C:8]1[N:13]=[CH:12][C:11](/[CH:14]=[CH:15]/[C:16]([N:18]([CH3:30])[CH2:19][C:20]2[N:21]([CH3:29])[C:22]3[C:27]([CH:28]=2)=[CH:26][CH:25]=[CH:24][CH:23]=3)=[O:17])=[CH:10][CH:9]=1.[NH3:31]>>[CH3:30][N:18]([CH2:19][C:20]1[N:21]([CH3:29])[C:22]2[C:27]([CH:28]=1)=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:16](/[CH:15]=[CH:14]/[C:11]1[CH:10]=[CH:9][C:8]([NH:3][C:4](=[O:7])[CH2:5][CH2:6][C:2]([NH2:31])=[O:1])=[N:13][CH:12]=1)=[O:17]

Participants

3

Conditions

Temperature
60 °C

Procedure

A mixture of (E)-3-[6-(2,5-dioxo-pyrrolidin-1-yl)pyridin-3-yl]-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)acrylamide (260 mg, 0.645 mmol) and ammonia (12 mL of 0.5M solution in 1,4-dioxane, 6.0 mmol) in a sealed tube was heated to 60° C. overnight. After cooling to ambient temperature, the resulting white precipitate was collected by filtration. The resulting solid was triturated with MeOH, washed with Et2O, and dried under high vacuum at 50° C. for 2 d to give the title compound (140 mg, 52%) as a white solid and as a mixture of amide rotamers: mp 225-227° C.; 1H NMR (300 MHz, DMSO-d6) δ 10.67-10.63 (m, 1H), 8.62-8.58 (m, 1H), 8.21-8.07 (m, 2H), 7.60-7.25 (m, 5H), 7.12 (dd, J=7.7, 7.4 Hz, 1H), 7.00 (dd, J=7.3, 6.9 Hz, 1H), 6.77 (br s, 1H), 6.42-6.17 (m, 1H), 5.05-4.85 (m, 2H), 3.72-3.68 (m, 3H), 3.12-2.99 (m, 3H), 2.64-2.60 (m, 2H), 2.40-2.36 (m, 2H); MS (ESI) m/e 420 (M+H)+.

Workup

  1. temperatureAfter cooling to ambient temperature
  2. filtrationthe resulting white precipitate was collected by filtration
  3. customThe resulting solid was triturated with MeOH
  4. washwashed with Et2O
  5. customdried under high vacuum at 50° C. for 2 d

Sources & evidence

ORD record
ord-a1c4d8a19a8e4d5db4b5fbb774ea6fa9
Source dataset
uspto-grants-2011_02
Patent number
US07879872B2

Reaction notes

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